Hollister, Inc.
FDA 510(k) & PMA Approved Devices — 85 products
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Total Devices85
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K123804 | INSTAFLO BOWEL CATHETER SYSTEM KIT | KNT | 2013-04-17 | View |
| 510(k) | K100273 | INSTAFLO BOWEL CATHETER SYSTEM KIT | KNT | 2010-04-22 | View |
| 510(k) | K090960 | VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184, | GBM | 2009-08-20 | View |
| 510(k) | K083153 | ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007 | KNT | 2009-02-04 | View |
| 510(k) | K050483 | EVADRI BLADDER CONTROL SYSTEMS | KPI | 2005-04-12 | View |
| 510(k) | K040779 | RESTORE WOUND CLEANSER | KMF | 2004-05-17 | View |
| 510(k) | K013612 | INCARE PELVIC FLOOR THERAPY SYSTEM | HIR | 2002-03-19 | View |
| 510(k) | K013653 | INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE | HIR | 2002-03-05 | View |
| 510(k) | K013483 | INCARE ADVANCE; INTERMITTENT CATHETER, PLUS INTERMITTENT CATHETER, PLUS KIT | KOD | 2002-01-14 | View |
| 510(k) | K013345 | INCARE INTERMITTENT CATHETER | KOD | 2002-01-07 | View |
| 510(k) | K013141 | MICROGYN PLUS STIMULATION DEVICE | KPI | 2001-12-19 | View |
| 510(k) | K011519 | AMEDA HYGIENIKIT | HGY | 2001-08-15 | View |
| 510(k) | K991214 | SIMPLICARE TRANSPARENT WOUND DRESSING | MGP | 1999-10-14 | View |
| 510(k) | K990456 | ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP | KPI | 1999-03-25 | View |
| 510(k) | K980976 | AMEDA DISPOSABLE VACUUM ASSIST CUP WITH FLUID RETENTION TRAP | HDB | 1998-08-21 | View |
| 510(k) | K980209 | SIMPLICARE THIN FILM WOUND DRESSINGS | MGP | 1998-02-20 | View |
| 510(k) | K974048 | INCARE PELVIC FLOOR THERAPY SYSTEM WITH DESKTOP COMPUTER | KPI | 1997-12-23 | View |
| 510(k) | K973023 | INCARE HOT/ICE SYSTEM FOOT/ANKLE BLANKET | ILO | 1997-11-03 | View |
| 510(k) | K971541 | VAGINAL 2 ELECTRODE STIMULATION/EMG PROBE - TAMPON | KPI | 1997-06-25 | View |
| 510(k) | K970602 | VAGINAL 2 ELECTRODE STIMULATION/EMG PROBE-SMALL | KPI | 1997-04-15 | View |
No matching devices.
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